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Octapharma AG

Group Associate Project Manager (m/f/d) - Quality Control

full-time•Vienna

Summary

Location

Vienna

Type

full-time

Experience

2-5 years

Company links

WebsiteLinkedInLinkedIn

About this role

Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation.

 

With over 1600 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location. 
 

This position is limited until 01.02.2028.

 

Your main tasks and responsibilities  

 

  • Manage and coordinate complex, cross-functional projects within the global QC network, ensuring timely delivery and alignment with corporate objectives
  • Develop project plans, define milestones, allocate resources, and monitor progress to ensure successful implementation
  • Collaborate with internal stakeholders across global functions and manufacturing sites to ensure seamless project execution
  • Identify risks and implement mitigation strategies to ensure operational excellence
  • Drive continuous improvement initiatives within QC processes and systems
  • Prepare and deliver clear, structured communication to senior management and project teams
  • Support global harmonization efforts and contribute to strategic decision-making in QC 

 

Your expertise and ideal skill set 

 

  • University degree in a scientific discipline (Master preferred)
  • Good understanding of analytical laboratory processes in the biopharmaceutical or life sciences field
  • Experience in pharmaceutical or biotechnological industry, global exposure is an asset
  • Project management skills  and advanced proficiency in Microsoft Office and project management tools
  • Excellent written and verbal communication skills in English
  • Ability to manage multiple priorities and work effectively under pressure
  • Willingness to travel as required by project needs
     

Your department - where you make an impact  
 

  • We, the Corporate Quality department, provides strategic alignment across local Quality Control departments, analytical method validation, and stability studies, ensuring efficient processes and regulatory compliance.



Thrive with us

 

  • Company restaurant & meal subsidy 
  • Training & further education 
  • Health promotion 
  • Parking spaces and good public transport connections  
  • Company and team events 

Enjoy these attractive benefits! You can find all offers here: Benefits

The minimum gross salary according to the collective agreement (chemical industry) is EUR 4.270,14 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary.  


It´s in our blood

We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.  

Do you have any questions? Then get in touch with your contact person. 

Mrs. Johanna Proksch, MA

Octapharma Pharmazeutika Produktionsges.m.b.H. 

Oberlaaer Straße 235, 1100 Wien 

T: +43 (1) 610 32 - 4299


Want to find out more about us? 

 
Visit our website Octapharma Career and follow us daily on LinkedIn.  

 

What you'll do

  • Manage and coordinate complex, cross-functional projects within the global QC network, ensuring timely delivery and alignment with corporate objectives. Collaborate with internal stakeholders to ensure seamless project execution and drive continuous improvement initiatives within QC processes.

About Octapharma AG

Octapharma is the world's largest privately-owned, independent company specializing in the field of blood plasma fractionation. With over 11,000 employees, we lead in the development and production of essential human proteins derived from human plasma and human cell lines. We support the treatment of patients in 118 countries with products across three therapeutic areas: Immunotherapy, Hematology, and Critical Care. Octapharma has seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany and Sweden, and operates more than 190 plasma donation centers across Europe and the US. Out sites in Germany: šŸ“ Octapharma Produktionsgesellschaft Deutschland mbH, Springe šŸ“ Octapharma Dessau GmbH, Dessau šŸ“ Octapharma Biopharmaceuticals GmbH, Heidelberg, Frankfurt, Berlin šŸ“ Octapharma GmbH, Langenfeld šŸ“ Octapharma Plasma GmbH, Langenfeld Community guidelines: https://bit.ly/3M8ioml

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Frequently Asked Questions

What does a Group Associate Project Manager (m/f/d) - Quality Control do at Octapharma AG?

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As a Group Associate Project Manager (m/f/d) - Quality Control at Octapharma AG, you will: manage and coordinate complex, cross-functional projects within the global QC network, ensuring timely delivery and alignment with corporate objectives. Collaborate with internal stakeholders to ensure seamless project execution and drive continuous improvement initiatives within QC processes..

Is the Group Associate Project Manager (m/f/d) - Quality Control position at Octapharma AG remote?

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The Group Associate Project Manager (m/f/d) - Quality Control position at Octapharma AG is based in Vienna, Austria. Contact the company through Clera for specific work arrangement details.

How do I apply for the Group Associate Project Manager (m/f/d) - Quality Control position at Octapharma AG?

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